Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 13, 2026, FDA's public records list Fiber Imaging Technologies with 5 510(k) clearances. The most recent is a 510(k) clearance dated Nov 5, 1999: COLDLIGHTSOURCE PL3000.
| Date | Record | Source |
|---|---|---|
| Nov 5, 1999 | COLDLIGHTSOURCE PL3000K993300 · FCW | 510(k) clearances |
| Oct 13, 1999 | URETERO-RENOSCOPEK992527 · FGB | 510(k) clearances |
| Sep 14, 1999 | SCHOELLY RIGID ENDOSCOPESK992437 · GCJ | 510(k) clearances |
| Aug 6, 1999 | FLEXISCOPE II ARTHROSCOPES AND ACCESSORIESK992040 · HRX | 510(k) clearances |
| Jul 13, 1999 | NASO-LARYNGO-PHARYNGOSCOPEK991560 · EOB | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
